Cardiovascular Efficacy and Safety of Bococizumab in High-Risk Patients

In two randomized trials comparing the PCSK9 inhibitor bococizumab with placebo, bococizumab had no benefit with respect to major adverse cardiovascular events in the lower-risk group but did have a significant benefit in the higher-risk group. Monoclonal antibodies that inhibit proprotein convertas...

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Veröffentlicht in:The New England journal of medicine 2017-04, Vol.376 (16), p.1527-1539
Hauptverfasser: Ridker, Paul M, Revkin, James, Amarenco, Pierre, Brunell, Robert, Curto, Madelyn, Civeira, Fernando, Flather, Marcus, Glynn, Robert J, Gregoire, Jean, Jukema, J. Wouter, Karpov, Yuri, Kastelein, John J.P, Koenig, Wolfgang, Lorenzatti, Alberto, Manga, Pravin, Masiukiewicz, Urszula, Miller, Michael, Mosterd, Arend, Murin, Jan, Nicolau, Jose C, Nissen, Steven, Ponikowski, Piotr, Santos, Raul D, Schwartz, Pamela F, Soran, Handrean, White, Harvey, Wright, R. Scott, Vrablik, Michal, Yunis, Carla, Shear, Charles L, Tardif, Jean-Claude
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Sprache:eng
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Zusammenfassung:In two randomized trials comparing the PCSK9 inhibitor bococizumab with placebo, bococizumab had no benefit with respect to major adverse cardiovascular events in the lower-risk group but did have a significant benefit in the higher-risk group. Monoclonal antibodies that inhibit proprotein convertase subtilisin–kexin type 9 (PCSK9) lower levels of plasma low-density lipoprotein (LDL) cholesterol and are promising agents for vascular risk reduction. 1 Patients who have received the fully human monoclonal antibodies evolocumab and alirocumab, for example, have had reductions in cardiovascular events in preliminary analyses; these drugs are under evaluation in large-scale trials involving patients with known cardiovascular disease. 2 , 3 Bococizumab is a third inhibitor of PCSK9 that, unlike evolocumab and alirocumab, is a humanized monoclonal antibody in which approximately 3% of the murine sequence remains in the antigen-binding complementarity-determining region. As part of the Studies . . .
ISSN:0028-4793
1533-4406
DOI:10.1056/NEJMoa1701488